Canonical Allele Identifier: CA1883385239
Community Standard Title: NM_000093.5(COL5A1):c.3852+224G=
Gene: COL5A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134812936G= , CM000671.2:g.134812936G= GRCh38
NC_000009.11:g.137704782G= , CM000671.1:g.137704782G= GRCh37
NC_000009.10:g.136844603G= NCBI36
NG_008030.1:g.176131G=

Transcript Alleles

HGVS Amino-acid Change
NM_000093.5:c.3852+224G= MANE Select NP_000084.3:n.3852+224G=
ENST00000371817.8:c.3852+224G= MANE Select ENSP00000360882.3:n.3852+224G=
NM_000093.4:c.3852+224G= NP_000084.3:n.3852+224G=
NM_001278074.1:c.3852+224G= NP_001265003.1:n.3852+224G=
ENST00000371817.7:c.3852+224G= ENSP00000360882.3:n.3852+224G=
ENST00000371820.4:c.3852+224G= ENSP00000360885.4:n.3852+224G=
ENST00000618395.4:c.3852+224G= ENSP00000481360.1:n.3852+224G=
XM_017014266.2:c.3852+224G= XP_016869755.1:n.3852+224G=
XR_001746183.1:n.4250+224G=
XR_929712.1:n.4254+224G=
XR_929713.1:n.4254+224G=